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RNAsnoop: efficient target prediction for H/ACA snoRNAs

  1. Peter F. Stadler1–6
  1. 1 Institute for Theoretical Chemistry, University of Vienna, Währingerstrasse 17, A-1090 Vienna, Austria, 2 Bioinformatics Group, Department of Computer Science, 3 Interdisciplinary Center for Bioinformatics, University of Leipzig, Härtelstrasse 16-18, D-04107 Leipzig, 4 Max Planck Institute for Mathematics in the Sciences, Inselstrasse 22, 5 RNomics Group, Fraunhofer Institut for Cell Therapy and Immunology, Perlikstraße 1,D-04103 Leipzig, Germany and 6 The Santa Fe Institute, 1399 Hyde Park Rd., Santa Fe, NM, USA
  1. * To whom correspondence should be addressed.
  • Received August 26, 2009.
  • Revision received November 30, 2009.
  • Accepted December 6, 2009.

Abstract

Motivation: Small nucleolar RNAs are an abundant class of non-coding RNAs that guide chemical modifications of rRNAs, snRNAs and some mRNAs. In the case of many ‘orphan’ snoRNAs, the targeted nucleotides remain unknown, however. The box H/ACA subclass determines uridine residues that are to be converted into pseudouridines via specific complementary binding in a well-defined secondary structure configuration that is outside the scope of common RNA (co-)folding algorithms.

Results: RNAsnoop implements a dynamic programming algorithm that computes thermodynamically optimal H/ACA-RNA interactions in an efficient scanning variant. Complemented by an support vector machine (SVM)-based machine learning approach to distinguish true binding sites from spurious solutions and a system to evaluate comparative information, it presents an efficient and reliable tool for the prediction of H/ACA snoRNA target sites. We apply RNAsnoop to identify the snoRNAs that are responsible for several of the remaining ‘orphan’ pseudouridine modifications in human rRNAs, and we assign a target to one of the five orphan H/ACA snoRNAs in Drosophila.

Availability: The C source code of RNAsnoop is freely available at http://www.tbi.univie.ac.at/∼htafer/RNAsnoop

Contact: htafer{at}tbi.univie.ac.at

Supplementary information: Supplementary data are available at Bioinformatics online.

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